HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 8-Acetyl-6-bromo-2,2,4,4-tetramethyl chroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 6-Bromo-2,2,4,4-tetramethylchroman | HCID 12137005 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-Acetyl-6-bromo-2,2,4,4-tetramethyl chroman | HCID 21107239 | 67% |
Reaction Steps
A stirred, cooled (−78° C.) solution of 6-bromo-2,2,4,4-tetramethyl chroman (1 g, 3.72 mol) in anhydrous dichloromethane (10 mol) was treated with aluminum chloride (0.8 g, 6.8 mol) followed by acetyl chloride (0.4 mol, 6.08 mol). After 10 minutes, the reaction mixture was diluted with water and extracted with diethyl ether. The organic phase was washed with water, and dried over anhydrous sodium sulfate, filtered and evaporated to a residue that was subjected to flash column chromatography on silica gel (230-400 mesh) using 10% ethyl acetate in hexane as the eluent to afford the title compound as a solid (0.78 g, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468391B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-73add12814054bf19e319dadea78c7fc |
| Source note | uspto-grants-2008_12 |